{"title":"Tau here, tau there, tau almost everywhere: Clarifying the distribution of tau in the adult CNS","authors":"Nicholas M. Kanaan","doi":"10.1002/cm.21820","DOIUrl":null,"url":null,"abstract":"<p>The microtubule-associated protein tau has gained significant attention over the last several decades primarily due to its apparent role in the pathogenesis of several diseases, most notably Alzheimer's disease. While the field has focused largely on tau's potential contributions to disease mechanisms, comparably less work has focused on normal tau physiology. Moreover, as the field has grown, some misconceptions and dogmas regarding normal tau physiology have become engrained in the traditional narrative. Here, one of the most common misconceptions regarding tau, namely its normal cellular/subcellular distribution in the CNS, is discussed. The literature describing the presence of tau in neuronal somata, dendrites, axons and synapses, as well as in glial cells is described. The origins for the erroneous description of tau as an “axon-specific,” “axon-enriched” and/or “neuron-specific” protein are discussed as well. The goal of this work is to help address these specific dogmatic misconceptions and provide a concise description of tau's normal cellular/subcellular localization in the adult CNS. This information can help refine our collective understanding of- and hypotheses about tau biology and pathobiology.</p>","PeriodicalId":55186,"journal":{"name":"Cytoskeleton","volume":"81 1","pages":"107-115"},"PeriodicalIF":2.4000,"publicationDate":"2023-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cm.21820","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cytoskeleton","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cm.21820","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The microtubule-associated protein tau has gained significant attention over the last several decades primarily due to its apparent role in the pathogenesis of several diseases, most notably Alzheimer's disease. While the field has focused largely on tau's potential contributions to disease mechanisms, comparably less work has focused on normal tau physiology. Moreover, as the field has grown, some misconceptions and dogmas regarding normal tau physiology have become engrained in the traditional narrative. Here, one of the most common misconceptions regarding tau, namely its normal cellular/subcellular distribution in the CNS, is discussed. The literature describing the presence of tau in neuronal somata, dendrites, axons and synapses, as well as in glial cells is described. The origins for the erroneous description of tau as an “axon-specific,” “axon-enriched” and/or “neuron-specific” protein are discussed as well. The goal of this work is to help address these specific dogmatic misconceptions and provide a concise description of tau's normal cellular/subcellular localization in the adult CNS. This information can help refine our collective understanding of- and hypotheses about tau biology and pathobiology.
过去几十年来,微管相关蛋白 tau 引起了人们的极大关注,这主要是因为它在几种疾病(尤其是阿尔茨海默病)的发病机制中发挥了明显的作用。虽然这一领域主要关注的是 tau 对疾病机制的潜在贡献,但关注正常 tau 生理机能的工作却相对较少。此外,随着该领域的发展,一些关于正常tau生理学的误解和教条已在传统的叙述中根深蒂固。在此,我们将讨论关于 tau 最常见的误解之一,即它在中枢神经系统中的正常细胞/亚细胞分布。文献描述了 tau 在神经元体、树突、轴突和突触以及神经胶质细胞中的存在。此外,还讨论了将 tau 错误地描述为 "轴突特异性"、"轴突丰富性 "和/或 "神经元特异性 "蛋白质的起源。这项工作的目的是帮助解决这些特定的教条式误解,并提供有关 tau 在成人中枢神经系统中正常细胞/亚细胞定位的简明描述。这些信息有助于完善我们对 tau 生物学和病理生物学的集体理解和假设。
期刊介绍:
Cytoskeleton focuses on all aspects of cytoskeletal research in healthy and diseased states, spanning genetic and cell biological observations, biochemical, biophysical and structural studies, mathematical modeling and theory. This includes, but is certainly not limited to, classic polymer systems of eukaryotic cells and their structural sites of attachment on membranes and organelles, as well as the bacterial cytoskeleton, the nucleoskeleton, and uncoventional polymer systems with structural/organizational roles. Cytoskeleton is published in 12 issues annually, and special issues will be dedicated to especially-active or newly-emerging areas of cytoskeletal research.